Laura Crisponi

13.9k total citations
41 papers, 1.7k citations indexed

About

Laura Crisponi is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Laura Crisponi has authored 41 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Genetics and 10 papers in Oncology. Recurrent topics in Laura Crisponi's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), RNA Research and Splicing (10 papers) and Cytokine Signaling Pathways and Interactions (10 papers). Laura Crisponi is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), RNA Research and Splicing (10 papers) and Cytokine Signaling Pathways and Interactions (10 papers). Laura Crisponi collaborates with scholars based in Italy, United States and Germany. Laura Crisponi's co-authors include Manuela Uda, Giuseppe Pilia, Antonino Forabosco, Chris Ottolenghi, David Schlessinger, Antonio Cao, Manila Deiana, David Schlessinger, José Elías García and Wendy L. Kimber and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Annals of the New York Academy of Sciences.

In The Last Decade

Laura Crisponi

40 papers receiving 1.7k citations

Peers

Laura Crisponi

GENET

PHEOH

PPCH

Djurdjica Coss United States

Harry M. Charlton United Kingdom

Sadahiro Azuma Japan

Lawrence C. Layman United States

Beverly J. White United States

Penelope Feuillan United States

Rula Abbud United States

Yoshikatsu Uematsu Japan

Bai‐Lin Wu United States

Hyung‐Goo Kim United States

Djurdjica Coss United States

Laura Crisponi

688 ×0.7

404 ×0.4

GENET

381 ×0.8

PHEOH

537 ×1.5

74 ×0.5

PPCH

Citations per year, relative to Laura Crisponi Laura Crisponi (= 1×) peers Djurdjica Coss

Countries citing papers authored by Laura Crisponi

Since Specialization

Citations

This map shows the geographic impact of Laura Crisponi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Laura Crisponi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Crisponi more than expected).

Fields of papers citing papers by Laura Crisponi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura Crisponi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Laura Crisponi. The network helps show where Laura Crisponi may publish in the future.

Co-authorship network of co-authors of Laura Crisponi

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Crisponi. A scholar is included among the top collaborators of Laura Crisponi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laura Crisponi. Laura Crisponi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

D’Alatri, Lucia, Claudia Manfredi, Roberta Onesimo, et al.. (2025). Do Rare Genetic Conditions Exhibit a Specific Phonotype? A Comprehensive Description of the Vocal Traits Associated with Crisponi/Cold-Induced Sweating Syndrome Type 1. Genes. 16(8). 881–881. 1 indexed citations

Onesimo, Roberta, Valentina Giorgio, Chiara Leoni, et al.. (2024). Feeding and Nutritional Key Features of Crisponi/Cold-Induced Sweating Syndrome. Genes. 15(9). 1109–1109. 2 indexed citations

Caballero-Oteyza, Andrés, Laura Crisponi, Xiao Peng, et al.. (2023). GenIA, the Genetic Immunology Advisor database for inborn errors of immunity. Journal of Allergy and Clinical Immunology. 153(3). 831–843. 2 indexed citations

Loges, Niki T., Yvonne Nitschke, Inga M. Höben, et al.. (2020). Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual. Stem Cell Research. 46. 101820–101820. 1 indexed citations

Buers, Insa, Niki T. Loges, Yvonne Nitschke, et al.. (2020). Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line. Stem Cell Research. 46. 101855–101855.

Angius, Andrea, Paolo Uva, Manuela Oppo, et al.. (2019). Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses. Clinical Genetics. 95(5). 607–614. 9 indexed citations

Buers, Insa, Ivana Persico, Yvonne Nitschke, et al.. (2019). Crisponi/cold‐induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts. Clinical Genetics. 97(1). 209–221. 11 indexed citations

Uva, Paolo, Manuela Oppo, Ivana Persico, et al.. (2019). Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report. BMC Medical Genetics. 20(1). 16–16. 15 indexed citations

Marongiu, Mara, Manila Deiana, Andrea Sbardellati, et al.. (2016). Novel action of FOXL2 as mediator of Col1a2 gene autoregulation. Developmental Biology. 416(1). 200–211. 6 indexed citations

10.

Terracciano, Antonio, Maria Grazia Piras, Monia Lobina, et al.. (2011). Genetics of serum BDNF: Meta-analysis of the Val66Met and genome-wide association study. The World Journal of Biological Psychiatry. 14(8). 583–589. 59 indexed citations

11.

Terracciano, Antonio, Monia Lobina, Maria Grazia Piras, et al.. (2011). Neuroticism, Depressive Symptoms, and Serum BDNF. Psychosomatic Medicine. 73(8). 638–642. 66 indexed citations

12.

Meloni, Alessandra, Mara Marongiu, Francesca Chiappe, et al.. (2011). Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders. European Journal of Human Genetics. 19(5). 525–533. 32 indexed citations

13.

Marongiu, Mara, Manila Deiana, Alessandra Meloni, et al.. (2010). The Forkhead Transcription Factor Foxl2 Is Sumoylated in Both Human and Mouse: Sumoylation Affects Its Stability, Localization, and Activity. PLoS ONE. 5(3). e9477–e9477. 22 indexed citations

14.

Crisponi, Laura, et al.. (2010). Successful treatment of cold‐induced sweating in Crisponi syndrome and its possible mechanism of action. Developmental Medicine & Child Neurology. 52(5). 494–497. 13 indexed citations

15.

Palomba, Grazia, Angela Loi, Giovanna Piras, et al.. (2009). A role of BRCA1 and BRCA2germline mutations in breast cancer susceptibility within Sardinian population. BMC Cancer. 9(1). 245–245. 17 indexed citations

16.

Sanna, Serena, Fabio Busonero, Andrea Maschio, et al.. (2009). Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. Human Molecular Genetics. 18(14). 2711–2718. 98 indexed citations

17.

Ottolenghi, Chris, Manuela Uda, Laura Crisponi, et al.. (2006). Determination and stability of sex. BioEssays. 29(1). 15–25. 43 indexed citations

18.

Ottolenghi, Chris, Manuela Uda, Toshio Hamatani, et al.. (2004). Aging of Oocyte, Ovary, and Human Reproduction. Annals of the New York Academy of Sciences. 1034(1). 117–131. 67 indexed citations

19.

Crisponi, Laura, Manuela Uda, Manila Deiana, et al.. (2004). FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences. Genomics. 83(5). 757–764. 42 indexed citations

20.

Schlessinger, David, Luisa Herrera, Laura Crisponi, et al.. (2002). Genes and translocations involved in POF. American Journal of Medical Genetics. 111(3). 328–333. 109 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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